@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_head {
  this: np:hasAssertion dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_assertion;
    np:hasProvenance dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_provenance;
    np:hasPublicationInfo dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_assertion a np:Assertion .
  
  dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_provenance a np:Provenance .
  
  dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_assertion {
  miriam-gene:1390 a ncit:C16612 .
  
  lld:C0021390 a ncit:C7057 .
  
  dgn-gda:DGN2e5a88120028aa188c5929565211321f sio:SIO_000628 miriam-gene:1390, lld:C0021390;
    a sio:SIO_001121 .
}

dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_provenance {
  dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_assertion dcterms:description
      "[These results suggest that common variants of the CREM gene are involved in the genetic component conferring general susceptibility to IBD, whereas STAT4 appears to be more specifically associated with UC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:22019623;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP750269.RAnEZp8g05g2k9csmO2wTGYMWsiMVskv_tVqD1l4-J7_A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:34+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}